Disease Index

human disease

spectrum of conditions caused by HIV infection

lymphoma that is marked classically by the presence of Reed-Sternberg cells

human disease

human disease

congenital disorder of the nervous system

human disease

medical condition

autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb.

syndrome characterized by Potter sequence, heart defect, cleft palate, polydactyly, and skeletal defects

gamma-amino butyric acid metabolism disorder that is characterized by an excess of homocarnosine in the brain and has material basis in a deficiency of serum carnosinase in its ability to hydrolyze homocarnosine

amino acid metabolic disorder that involves an accumulation of homocysteine in the serum and an increased excretion of homocysteine in the urine

v1)

human disease

human disease

human disease

congenital disorder of urinary system

Tylosis with oesophageal cancer

a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.

human disease

human disease

disease